Transducer S7-2t 989605440772Recalls & reported problems
Philips Ultrasound LLC · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
4 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 4
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884838067646), received between Jun 19, 2020 and Jun 19, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Device” (1 report).
4 FDA recall records name this device's identifier, 4 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Sep 5, 2025Class IIIOpen, Classified
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Z-1624-2026 · Root cause: Device Design · Recall details · FDA record ↗
- Jul 3, 2025Class IIIOpen, Classified
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Z-2412-2025 · Root cause: Device Design · Recall details · FDA record ↗
- Jul 3, 2025Class IIIOpen, Classified
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Z-2396-2025 · Root cause: Device Design · Recall details · FDA record ↗
- May 28, 2025Class IIOpen, Classified
Ultrasound transducer devices were refurbished beyond their useful life.
Z-2059-2025 · Root cause: Process control · Recall details · FDA record ↗
Most reported problems
Device problems
- Defective Device1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 19, 2020Defective Device
A CUSTOMER REPORTED AN S7-2 OMNI MODEL TRANSDUCER WOULD NOT ARTICULATE DURING USE. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10176521 ↗
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- Transducer X8-2t 989605455171Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic8 recalls19 reports
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- Site~Rite 8 Ultrasound System 9770600YBard Access Systems, Inc. · System, imaging, pulsed echo, ultrasonic330 reports
- Transducer C9-2 989605391092Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic5 recalls0 reports
- Transducer S5-1 989605412082Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic5 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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